US6342081B1 - Cloud point depressants for middle distillate fuels - Google Patents

Cloud point depressants for middle distillate fuels Download PDF

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US6342081B1
US6342081B1 US09/592,491 US59249100A US6342081B1 US 6342081 B1 US6342081 B1 US 6342081B1 US 59249100 A US59249100 A US 59249100A US 6342081 B1 US6342081 B1 US 6342081B1
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fuel
cloud point
additive
polyimide
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Maged G. Botros
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Equistar Chemicals LP
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    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/18Organic compounds containing oxygen
    • C10L1/192Macromolecular compounds
    • C10L1/195Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • C10L1/196Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds derived from monomers containing a carbon-to-carbon unsaturated bond and a carboxyl group or salts, anhydrides or esters thereof homo- or copolymers of compounds having one or more unsaturated aliphatic radicals each having one carbon bond to carbon double bond, and at least one being terminated by a carboxyl radical or of salts, anhydrides or esters thereof
    • C10L1/1966Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds derived from monomers containing a carbon-to-carbon unsaturated bond and a carboxyl group or salts, anhydrides or esters thereof homo- or copolymers of compounds having one or more unsaturated aliphatic radicals each having one carbon bond to carbon double bond, and at least one being terminated by a carboxyl radical or of salts, anhydrides or esters thereof poly-carboxylic
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/22Organic compounds containing nitrogen
    • C10L1/234Macromolecular compounds
    • C10L1/236Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds derivatives thereof
    • C10L1/2364Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds derivatives thereof homo- or copolymers derived from unsaturated compounds containing amide and/or imide groups

Definitions

  • This invention relates to an improved fuel composition and fuel additives which are useful as cloud point depressants.
  • Distillate fuels such as diesel fuels tend to exhibit reduced flow at reduced temperatures. This reduced flow affects the transport and use of the distillate fuels not only in the refinery but also in an internal combustion engine. If the distillate fuel is cooled to below a temperature at which solid formation begins to occur in the fuel, generally known as the cloud point (ASTM D 2500) or wax appearance point (ASTM D 3117), solids forming in the fuel will essentially prevent the flow of the fuel, plugging piping in the refinery, during transport of the fuel, and in inlet lines supplying an engine. Under low temperature conditions during consumption of the distillate fuel, as in a diesel engine, wax precipitation and gelation can cause the engine fuel filter to plug.
  • distillate fuels encompass a range of fuel types, typically including but not limited to kerosene, intermediate distillates, lower volatility distillate gas oils, and higher viscosity distillates. Grades encompassed by the term include Grades No. 1-D, 2-D and 4-D for diesel fuels as defined in ASTM D 975, incorporated herein by reference.
  • the distillate fuels are useful in a range of applications, including use in automotive diesel engines and in non-automotive applications under both varying and relatively constant speed and load conditions.
  • the cloud point of a fuel is the temperature at which a cloud of wax crystals first appears in a liquid when it is cooled under conditions prescribed in the test method as defined in ASTM D 2500, incorporated herein by reference.
  • the cloud point behavior of a distillate fuel such as diesel fuel is a function of its composition.
  • the fuel is comprised of a mixture of hydrocarbons including normal paraffins, branched paraffins, olefins, aromatics and other non-polar and polar compounds. As the diesel fuel temperature decreases at the refinery, during transport, or in a vehicle, one or more components of the fuel will tend to separate, or precipitate.
  • the cloud point of the fuel is defined as the temperature at which the first waxes appear. The cloud point corresponds to an equilibrium state based on thermodynamic relationships which determine the solubility of paraffins in the diesel fuel.
  • Additives to decrease the cloud point also known as cloud point depressants, have been used in fuels to delay the formation of solid wax crystals and thereby aid in enhancing the operability of the fuel.
  • a cloud point depressant may also provide economic benefits in connection with the refining of the diesel fuel.
  • a cloud point depressant will typically lower the cloud point by 2 to 3° C. This lowering of the cloud point temperature by the depressant is known to compensate for the backing out of 20 to 30% of the kerosene fraction originally required to meet the cloud point specification.
  • the components of the diesel fuel having the lowest solubility tend to be the first to separate as solids from the fuel with decreasing temperature.
  • Straight chain hydrocarbons such as normal paraffins, generally have the lowest solubility in the diesel fuel.
  • the paraffin crystals which separate from the diesel fuel appear as individual crystals. As more crystals form in the fuel, they tend to agglomerate and eventually reach a particle size which becomes visible to the eye and creates a cloudy appearance.
  • additives into diesel fuel to enhance the flow properties of the fuel at low temperatures. These additives are generally viewed as operating under either or both of two primary mechanisms. In the first, the additive molecules have a configuration which allow them to interact with the n-paraffin molecules at the growing ends of the paraffin crystals. The interacting additive molecules by steric effects act as a cap to prevent additional paraffin molecules from adding to the crystal, thereby limiting the length of the existing crystal.
  • the flow modifying additive may improve the flow properties of diesel fuel at low temperatures by functioning as a nucleator to promote the growth of smaller size crystals.
  • Additional, secondary, mechanisms involving the modification of wax properties in the fuel by incorporation of additives include, but are not limited to, dispersal of the wax in the fuel and solubilization of the wax in the fuel.
  • the range of available diesel fuels includes Grade No. 2-D, defined in ASTM D 975-90 as a general purpose, middle distillate fuel for automotive diesel engines, which is also suitable for use in non-automotive applications, especially in conditions of frequently varying speed and load. Certain of these Grade No. 2-D (No. 2) fuels may be classified as being hard to treat when using one or more additives to improve flow.
  • a hard-to-treat diesel fuel is either unresponsive to a flow improving additive, or requires increased levels of one or more additives relative to a normal fuel to effect flow improvement.
  • Fuels in general, and diesel fuels in particular, are mixtures of hydrocarbons of different chemical types (i.e., paraffins, aromatics, olefins, etc.) wherein each type may be present in a range of molecular weights and carbon lengths.
  • the cloud point temperature is a function of one or more properties of the fuel, the properties being attributable to the composition of the fuel. These properties include the paraffin concentration of the fuel, the molecular weight of the paraffins, and the chemical nature of the non-paraffin part of the fuel.
  • the compositional properties which render a fuel hard to treat relative to normal fuels include a narrower wax distribution; the virtual absence of very high molecular weight waxes, or inordinately large amounts of very high molecular weight waxes; a higher total percentage of wax; and a higher average normal paraffin carbon number range. It is difficult to generate a single set of quantitative parameters which define a hard-to-treat fuel. Nevertheless, measured parameters which tend to identify a hard-to-treat middle distillate fuel include a temperature range of less than 100° C. between the 20% distilled and 90% distilled temperatures (as determined by test method ASTM D 86 incorporated herein by reference), a temperature range less than 25° C. between the 90% distilled temperature and the final boiling point (see ASTM D 86), and a final boiling point above or below the temperature range 360° to 380° C.
  • a fuel will cool to its cloud point generally in a static environment, but will also become cloudy in a dynamic environment such as a moving fuel tank at sufficiently low temperature.
  • additives which improve the cloud point characteristics of distillate fuels. Because additives are incorporated into the fuel to improve distinct characteristics of the fuel, it is possible that one additive may have an antagonistic effect on another additive. It is therefore desired that the cloud point additive not demonstrate an antagonism to the characteristics of the fuel as to one or more other properties, such as cold flow or wax anti-settling properties. Further, there remains a need for additive compositions which are capable of depressing the cloud point of hard-to-treat fuels.
  • Copending application Ser. No. 09/311,465 is directed to certain maleic anhydride ⁇ -olefin copolymer and polyimide additives incorporated into distillate fuel to improve the wax anti-settling properties of the fuel.
  • Copending application Ser. No.09/311,459 is directed to the combination of an ethylene vinyl acetate isobutylene terpolymer with one or more additive components including certain maleic anhydride ⁇ -olefin copolymer and polyimide components to effect cold flow improvement in distillate fuels.
  • the maleic anhydride olefin copolymer additive is prepared by the reaction of maleic anhydride with ⁇ -olefin. Generally this copolymer additive contains substantially equimolar amounts of maleic anhydride and ⁇ -olefin.
  • the operative starting ⁇ -olefin is a mixture of individual ⁇ -olefins having a range of carbon numbers.
  • the starting ⁇ -olefin composition used to prepare the maleic anhydride olefin copolymer additive of the invention has at least a minimum ⁇ -olefin concentration by weight with a carbon number within the range from about C 16 to about C 18 .
  • the additive generally does not contain ⁇ -olefin of a single carbon number; thus the additive consists of blends of ⁇ -olefins having carbon numbers within this range.
  • the operative starting ⁇ -olefin may have a minor component portion which is outside the above carbon number range.
  • the maleic anhydride ⁇ -olefin copolymers have a number average molecular weight in the range of about 700 to about 10,000 as measured by vapor pressure osmometry.
  • the invention also encompasses a cloud point depressant comprising a polyimide produced by the reaction of an alkyl amine, maleic anhydride and ⁇ -olefin.
  • a cloud point depressant comprising a polyimide produced by the reaction of an alkyl amine, maleic anhydride and ⁇ -olefin.
  • the polyimide is produced from substantially equimolar amounts of maleic anhydride and ⁇ -olefin.
  • the operative ⁇ -olefin is similar in composition to that described above for the maleic anhydride olefin copolymer additive, having a carbon number range from about C 16 to about C 18 .
  • Particularly advantageous cloud point depressant properties are obtained when the alkyl amine is tallow amine.
  • the polyimide has a number average molecular weight in the range of about 1,200 to about 10,000, preferably in the range of about 1,200 to about 5,000, as measured by vapor pressure osmometry.
  • the ethylene vinyl acetate isobutylene terpolymer additive has a weight average molecular weight in the range of about 1,500 to about 18,000, preferably about 3,000 to about 12,000; a number average molecular weight in the range of about 400 to about 3,000, preferably about 1,500 to about 2,500; and a ratio of weight average molecular weight to number average molecular weight from about 1.5 to about 6.
  • R has at least 80% by weight of a hydrocarbon substituent from about 14 to about 16 carbons, and n is from about 2 to about 30.
  • R has at least 90% by weight of a hydrocarbon substituent from about 14 to about 16 carbons, and most preferably R has at least 95% by weight of a hydrocarbon substrate from about 14 to about 16 carbons.
  • the resulting maleic anhydride ⁇ -olefin copolymer has a number average molecular weight in the range of about 700 to about 10,000, and preferably in the range of about 700 to about 4,000, as determined by vapor pressure osmometry.
  • the cloud point depressant additive of this invention typically encompasses a mixture of hydrocarbon substituents of varying carbon number within the recited range, and encompasses straight and branched chain moieties.
  • R has at least 80% by weight of a hydrocarbon substituent from about 14 to about 16 carbons
  • R′ has at least 80% by weight of a hydrocarbon substituent from 16 to 18 carbons
  • n is from about 2 to about 17, also has cloud point depressant properties.
  • R has at least 90% by weight of a hydrocarbon substituent from about 14 to about 16 carbons, and most preferably R has at least 95% by weight of a hydrocarbon substituent from about 14 to about 16 carbons.
  • R′ has at least 90% by weight of a hydrocarbon substituent from 16 to 18 carbons.
  • the above additive, described as a polyimide has a number average molecular weight as determined by vapor pressure osmometry in the range of about 1,200 to about 10,000, and preferably in the range of about 1,200 to about 5,000.
  • ethylene vinyl acetate isobutylene terpolymers demonstrate cloud point depressant properties both alone and in combination with one or more of the above maleic anhydride ⁇ -olefin copolymer or polyimide additives.
  • Useful ethylene vinyl acetate isobutylene terpolymers have a weight average molecular weight in the range of about 1,500 to about 18,000, a number average molecular weight in the range of about 400 to about 3,000, and a ratio of weight average molecular weight to number average molecular weight from about 1.5 to about 6.
  • the weight average molecular weight ranges from about 3,000 to about 12,000, and the number average molecular weight ranges from about 1,500 to about 2,500.
  • the terpolymers have a Brookfield viscosity in the range of about 100 to about 300 centipoise at 140° C. Typically the Brookfield viscosity is in the range of about 100 to about 200 centipoise.
  • Vinyl acetate content is from about 25 to about 55 weight percent. Preferably the vinyl acetate content ranges from about 30 to about 45 weight percent; more preferably the vinyl acetate content ranges from about 35 to about 45 weight percent.
  • the branching index is from 2 to 15, and preferably 5 to 10.
  • the rate of isobutylene introduction depends on the rate of vinyl acetate introduction, and may range from about 0.01 to about 10 times the rate of vinyl acetate monomer flow rate to the reactor.
  • a fuel will cool to its cloud point generally in a static environment, such as storage tanks, shipping tanks or even fuel tanks where no separate agitation is supplied. However, a fuel will become cloudy even in a dynamic environment such as a moving fuel tank at sufficiently low temperature.
  • ASTM D 2500 for measuring cloud point formation or ASTM D 3117 for measuring the wax appearance point both incorporated herein by reference, can be utilized.
  • the maleic anhydride ⁇ -olefin copolymer or polyimide can be combined with an ethylene vinyl acetate isobutylene terpolymer or ethylene vinyl acetate copolymer to produce a cloud point depressant additive combination which also provides cold flow improvement without adversely affecting the cloud point depressant properties.
  • the maleic anhydride ⁇ -olefin copolymer or polyimide additives of the present invention act as cloud point depressants when effective amounts are added to distillate fuels.
  • Useful amounts of the additives range from about 50 to about 1,500 ppm by weight of the fuel being treated.
  • Preferred amounts of the additives to improve cloud point depressant properties range from about 250 to about 500 ppm by weight of treated fuel.
  • Maleic anhydride ⁇ -olefin copolymers and polyimides used according to the teachings of this invention may be derived from ⁇ -olefin products such as those manufactured by Chevron Corporation and identified as Gulftene® 18 Alpha-Olefin, or the like.
  • Useful amounts of the terpolymers range from about 10 to about 1,000 ppm by weight of the fuel being treated. Preferred amounts of terpolymers range from about 25 to about 250 ppm by weight of treated fuel in connection with improving cloud point depression.
  • the additives of this invention may be used as the sole additive in a distillate fuel.
  • the polyimide or maleic anhydride ⁇ -olefin copolymers may be used in combination with one or more terpolymers or copolymers as described above.
  • cloud point depressant additives of this invention may be used in combination with other fuel additives such as corrosion inhibitors, antioxidants, sludge inhibitors, cold flow improvers, wax anti-settling agents, and the like.
  • the additive combinations described below were combined with a variety of diesel fuels at a weight concentration of about 50-1,500 ppm additive combination in the fuel, preferably 250-500 ppm additive combination in the fuel. Higher additive concentrations tend to impart additional cloud point depression effects to the fuel; however, the rate of improvement is lower at concentration levels above about 500 ppm when compared to the rate of improvement at levels below about 500 ppm.
  • the additive or additive combination was combined with the fuel from a concentrate. One part of a 1:1 weight mixture of additive and xylene was combined with 19 parts by weight of the fuel to be evaluated to prepare the concentrate. The actual final weight concentration of additive in the fuel was adjusted by varying the appropriate amount of the concentrate added to the fuel. If more than one additive was incorporated into the fuel, individual additive concentrates were mixed into the fuel substantially at the same time.
  • the ⁇ -olefin used in making the above additives is a mixture of individual ⁇ -olefins having a range of carbon numbers.
  • the starting ⁇ -olefin used to prepare both the maleic anhydride olefin copolymer and polyimide additives of the invention has at least a minimum concentration by weight which has a carbon number within the range from about C 16 to about C 18 .
  • the substituent “R” in the above formulas will have carbon numbers which are two carbons less than the ⁇ -olefin length, two of the ⁇ -olefin carbons becoming part of the polymer chain directly bonded to the repeating maleic anhydride or polyimide rings.
  • ⁇ -olefins are not manufactured to a single carbon chain length, and thus the manufactured product will consist of component portions of individual ⁇ -olefins of varying carbon chain length.
  • the substituent “R′” used in the polyimide cloud point additive will also have a minimum concentration within a range of carbon numbers.
  • Tallow amine is useful to introduce the R′ substituent in connection with polyimide manufacture, and is generally derived from tallow fatty acid.
  • the range and percentage of carbon numbers for the components of the tallow amine will generally be those of tallow fatty acid.
  • Tallow fatty acid is generally derived from beef tallow or mutton tallow. Though the constituent fatty acids may vary substantially in individual concentration in the beef tallow or mutton tallow based on factors such as source of the tallow, treatment and age of the tallow, general values have been generated and are provided in the table below. The values are typical rather than average.
  • the fatty acids from beef or mutton tallow can also be hydrogenated to lower the degree of unsaturation.
  • a tallow amine may contain a major portion by weight of unsaturated amine molecules, and alternatively with sufficient hydrogenation treatment may contain virtually no unsaturated amine molecules.
  • concentration by weight of hydrocarbon substituents from 16 to 18 carbons will be at least 80% by weight, and typically at least 90% by weight.
  • the following table lists maleic anhydride ⁇ -olefin copolymer and polyimide additives with their carbon number distributions for the various substituents of the additives tested.
  • the percentages by weight of the carbon number ranges for the starting ⁇ -olefins were determined by using a Hewlett Packard HP-5890 gas chromatograph with a Chrompack WCOT (wool coated open tubular) Ulti-Metal 10 m ⁇ 0.53 mm ⁇ 0.15 ⁇ m film thickness column, with an HT SIMDIST CB coating.
  • the sample was introduced via on-column injection onto the column as a solution in toluene.
  • the gas chromatograph was equipped with a hydrogen flame ionization detector.
  • copolymers and terpolymers utilized individually in preparing the various additive combinations are characterized in Table 2 set out below.
  • Fuels included in the evaluation of additives for cloud point depression performance are listed below in Table 3, which provides distillation data for the respective fuels according to test method ASTM D 86.
  • the data indicate the boiling point temperature (° C.) at which specified volume percentages of the fuel have been recovered from the original pot contents at atmospheric pressure.
  • the fuel met at least one of the above three evaluation parameters, i.e., 90%-20% distilled temperature difference, 90%-final boiling point distilled temperature difference, or final boiling point, it was considered hard to treat. Based on the evaluation parameters and the data in Tables 3 and 4, fuels 1 through 8 and 10 are considered hard to treat, and fuel 9 is considered normal. As the following examples demonstrate, the cloud point additives of the invention have beneficial effects when used with both normal and hard-to-treat fuels.
  • the cloud points of three fuel compositions were compared.
  • the fuel used in preparing each of the compositions was Fuel 1.
  • the first fuel composition contained no added cloud point depressant.
  • the second fuel composition included 500 ppm by weight of Polyimide I.
  • the third fuel composition included 500 ppm by weight of Maleic Copolymer I. The results are set out in Table 5.
  • Example 2 The effect of change in concentration of cloud point depressant additive on the cloud point was evaluated using Fuel 2.
  • the two additives tested above in Example 1 were separately combined with Fuel 2 and evaluated for cloud point depressant effect at additive concentrations of 500 ppm and 1000 ppm by weight.
  • the cloud point temperatures are set out in Table 6.
  • incorporation of a terpolymer additive to the respective fuels resulted in a demonstrable cloud point depressant effect.
  • incorporation of a copolymer additive either had the undesirable effect of raising the cloud point, or of providing a less substantial positive effect on cloud point depression compared to the terpolymer additives tested.
  • the effect of one additive may not positively correlate to that of another additive.
  • an additive incorporated to improve one property of a fuel may have an adverse effect on another property of the fuel.
  • an ethylene vinyl acetate copolymer or an ethylene vinyl acetate isobutylene terpolymer which can be used to improve the cold flow properties of the fuel, combined with a polyimide or maleic anhydride ⁇ -olefin copolymer of the invention generally does not have an antagonistic effect on either the cloud point or cold flow characteristics of the fuel.
  • an additive package consisting of 500 ppm by weight of a 1:1 mixture of either copolymer or terpolymer and polyimide I was combined with a variety of fuels and measured for cloud point depression.
  • the additive package combinations and cloud point measurements are set out in Table 11 below.
  • the pour point of Fuel 2 was ⁇ 21° C. without additive. Incorporation of 250 ppm Copolymer I and 500 ppm Polyimide I improved the pour point to ⁇ 44° C., and incorporation of 250 ppm Terpolymer I and 500 ppm Polyimide I improved the pour point to ⁇ 50° C.
  • LTFT Low Temperature Flow Test
  • the additives of the invention provide substantial improvements in the cloud point properties of distillate fuels relative to the unmodified fuel.
  • the improvement in cloud point depression extends to both normal and hard-to-treat fuels.
  • These additives may be used in combination with other fuel additives, such as those for improving flow properties to enhance the operability of the fuel by encompassing the cloud point depression improvement as well as the properties improved by incorporation of the other additives.

Abstract

An additive for distillate and a fuel composition having improved cloud point depressant properties. The additive is incorporated into a major proportion of distillate fuel and is a maleic anhydride α-olefin copolymer or a polyimide having the following structure:
Figure US06342081-20020129-C00001
wherein R has at least 80% by weight of a hydrocarbon substituent from about 14 to about 16 carbons, X is oxygen or
Figure US06342081-20020129-C00002
wherein N is nitrogen and R′ has at least 80% by weight of a hydrocarbon substituent from 16 to 18 carbons, and n is from about 2 to about 30 when X is oxygen, and from about 2 to about 17 when X is
Figure US06342081-20020129-C00003
Alternatively, the cloud point additive can be an ethylene vinyl acetate isobutylene terpolymer.

Description

This is a division of application Ser. No. 09/351,652, filed Jul. 13, 1999 now U.S. Pat. No. 6,143,043.
FIELD OF THE INVENTION
This invention relates to an improved fuel composition and fuel additives which are useful as cloud point depressants.
BACKGROUND OF THE INVENTION
Distillate fuels such as diesel fuels tend to exhibit reduced flow at reduced temperatures. This reduced flow affects the transport and use of the distillate fuels not only in the refinery but also in an internal combustion engine. If the distillate fuel is cooled to below a temperature at which solid formation begins to occur in the fuel, generally known as the cloud point (ASTM D 2500) or wax appearance point (ASTM D 3117), solids forming in the fuel will essentially prevent the flow of the fuel, plugging piping in the refinery, during transport of the fuel, and in inlet lines supplying an engine. Under low temperature conditions during consumption of the distillate fuel, as in a diesel engine, wax precipitation and gelation can cause the engine fuel filter to plug.
As used herein, distillate fuels encompass a range of fuel types, typically including but not limited to kerosene, intermediate distillates, lower volatility distillate gas oils, and higher viscosity distillates. Grades encompassed by the term include Grades No. 1-D, 2-D and 4-D for diesel fuels as defined in ASTM D 975, incorporated herein by reference. The distillate fuels are useful in a range of applications, including use in automotive diesel engines and in non-automotive applications under both varying and relatively constant speed and load conditions.
The cloud point of a fuel is the temperature at which a cloud of wax crystals first appears in a liquid when it is cooled under conditions prescribed in the test method as defined in ASTM D 2500, incorporated herein by reference. The cloud point behavior of a distillate fuel such as diesel fuel is a function of its composition. The fuel is comprised of a mixture of hydrocarbons including normal paraffins, branched paraffins, olefins, aromatics and other non-polar and polar compounds. As the diesel fuel temperature decreases at the refinery, during transport, or in a vehicle, one or more components of the fuel will tend to separate, or precipitate. The cloud point of the fuel is defined as the temperature at which the first waxes appear. The cloud point corresponds to an equilibrium state based on thermodynamic relationships which determine the solubility of paraffins in the diesel fuel.
Additives to decrease the cloud point, also known as cloud point depressants, have been used in fuels to delay the formation of solid wax crystals and thereby aid in enhancing the operability of the fuel. In addition, a cloud point depressant may also provide economic benefits in connection with the refining of the diesel fuel. To reach a particular cloud point specification, a certain amount of hydrocarbons in the kerosene boiling range are left in the diesel fuel fraction. A cloud point depressant will typically lower the cloud point by 2 to 3° C. This lowering of the cloud point temperature by the depressant is known to compensate for the backing out of 20 to 30% of the kerosene fraction originally required to meet the cloud point specification.
The components of the diesel fuel having the lowest solubility tend to be the first to separate as solids from the fuel with decreasing temperature. Straight chain hydrocarbons, such as normal paraffins, generally have the lowest solubility in the diesel fuel. Generally, the paraffin crystals which separate from the diesel fuel appear as individual crystals. As more crystals form in the fuel, they tend to agglomerate and eventually reach a particle size which becomes visible to the eye and creates a cloudy appearance.
It is known to incorporate additives into diesel fuel to enhance the flow properties of the fuel at low temperatures. These additives are generally viewed as operating under either or both of two primary mechanisms. In the first, the additive molecules have a configuration which allow them to interact with the n-paraffin molecules at the growing ends of the paraffin crystals. The interacting additive molecules by steric effects act as a cap to prevent additional paraffin molecules from adding to the crystal, thereby limiting the length of the existing crystal.
In the second mechanism, the flow modifying additive may improve the flow properties of diesel fuel at low temperatures by functioning as a nucleator to promote the growth of smaller size crystals.
Additional, secondary, mechanisms involving the modification of wax properties in the fuel by incorporation of additives include, but are not limited to, dispersal of the wax in the fuel and solubilization of the wax in the fuel.
The range of available diesel fuels includes Grade No. 2-D, defined in ASTM D 975-90 as a general purpose, middle distillate fuel for automotive diesel engines, which is also suitable for use in non-automotive applications, especially in conditions of frequently varying speed and load. Certain of these Grade No. 2-D (No. 2) fuels may be classified as being hard to treat when using one or more additives to improve flow. A hard-to-treat diesel fuel is either unresponsive to a flow improving additive, or requires increased levels of one or more additives relative to a normal fuel to effect flow improvement.
Fuels in general, and diesel fuels in particular, are mixtures of hydrocarbons of different chemical types (i.e., paraffins, aromatics, olefins, etc.) wherein each type may be present in a range of molecular weights and carbon lengths. The cloud point temperature is a function of one or more properties of the fuel, the properties being attributable to the composition of the fuel. These properties include the paraffin concentration of the fuel, the molecular weight of the paraffins, and the chemical nature of the non-paraffin part of the fuel. For example, in the case of a hard-to-treat fuel the compositional properties which render a fuel hard to treat relative to normal fuels include a narrower wax distribution; the virtual absence of very high molecular weight waxes, or inordinately large amounts of very high molecular weight waxes; a higher total percentage of wax; and a higher average normal paraffin carbon number range. It is difficult to generate a single set of quantitative parameters which define a hard-to-treat fuel. Nevertheless, measured parameters which tend to identify a hard-to-treat middle distillate fuel include a temperature range of less than 100° C. between the 20% distilled and 90% distilled temperatures (as determined by test method ASTM D 86 incorporated herein by reference), a temperature range less than 25° C. between the 90% distilled temperature and the final boiling point (see ASTM D 86), and a final boiling point above or below the temperature range 360° to 380° C.
A fuel will cool to its cloud point generally in a static environment, but will also become cloudy in a dynamic environment such as a moving fuel tank at sufficiently low temperature. There continues to be a demand for additives which improve the cloud point characteristics of distillate fuels. Because additives are incorporated into the fuel to improve distinct characteristics of the fuel, it is possible that one additive may have an antagonistic effect on another additive. It is therefore desired that the cloud point additive not demonstrate an antagonism to the characteristics of the fuel as to one or more other properties, such as cold flow or wax anti-settling properties. Further, there remains a need for additive compositions which are capable of depressing the cloud point of hard-to-treat fuels.
SUMMARY OF THE INVENTION
It has been found that certain polyimide and maleic anhydride olefin polymer additives with carbon substituent chain lengths within a specified range, and alternatively certain ethyl vinyl acetate isobutylene terpolymers will depress the cloud point of certain distillate fuels such as No. 2 diesel fuel. Also, the above polyimide and maleic anhydride olefin polymer additives in combination with other materials such as ethylene vinyl acetate isobutylene terpolymers demonstrate substantial improvement in depressing the cloud point of certain distillate fuels when incorporated therein. With the latter additive combinations the cold flow properties of the distillate fuels are not adversely affected by the incorporation of the polyimide or maleic anhydride olefin polymer additive.
Copending application Ser. No. 09/311,465 is directed to certain maleic anhydride α-olefin copolymer and polyimide additives incorporated into distillate fuel to improve the wax anti-settling properties of the fuel. Copending application Ser. No.09/311,459 is directed to the combination of an ethylene vinyl acetate isobutylene terpolymer with one or more additive components including certain maleic anhydride α-olefin copolymer and polyimide components to effect cold flow improvement in distillate fuels.
The maleic anhydride olefin copolymer additive is prepared by the reaction of maleic anhydride with α-olefin. Generally this copolymer additive contains substantially equimolar amounts of maleic anhydride and α-olefin. The operative starting α-olefin is a mixture of individual α-olefins having a range of carbon numbers. The starting α-olefin composition used to prepare the maleic anhydride olefin copolymer additive of the invention has at least a minimum α-olefin concentration by weight with a carbon number within the range from about C16 to about C18. The additive generally does not contain α-olefin of a single carbon number; thus the additive consists of blends of α-olefins having carbon numbers within this range. The operative starting α-olefin may have a minor component portion which is outside the above carbon number range. The maleic anhydride α-olefin copolymers have a number average molecular weight in the range of about 700 to about 10,000 as measured by vapor pressure osmometry.
The invention also encompasses a cloud point depressant comprising a polyimide produced by the reaction of an alkyl amine, maleic anhydride and α-olefin. Generally the polyimide is produced from substantially equimolar amounts of maleic anhydride and α-olefin. The operative α-olefin is similar in composition to that described above for the maleic anhydride olefin copolymer additive, having a carbon number range from about C16 to about C18. Particularly advantageous cloud point depressant properties are obtained when the alkyl amine is tallow amine. The polyimide has a number average molecular weight in the range of about 1,200 to about 10,000, preferably in the range of about 1,200 to about 5,000, as measured by vapor pressure osmometry.
The ethylene vinyl acetate isobutylene terpolymer additive has a weight average molecular weight in the range of about 1,500 to about 18,000, preferably about 3,000 to about 12,000; a number average molecular weight in the range of about 400 to about 3,000, preferably about 1,500 to about 2,500; and a ratio of weight average molecular weight to number average molecular weight from about 1.5 to about 6.
DETAILED DESCRIPTION OF THE INVENTION
It has been found that unexpectedly advantageous cloud point depressing properties can be imparted to distillate fuels by incorporating an additive having the following structure:
Figure US06342081-20020129-C00004
wherein R has at least 80% by weight of a hydrocarbon substituent from about 14 to about 16 carbons, and n is from about 2 to about 30. Preferably R has at least 90% by weight of a hydrocarbon substituent from about 14 to about 16 carbons, and most preferably R has at least 95% by weight of a hydrocarbon substrate from about 14 to about 16 carbons. The resulting maleic anhydride α-olefin copolymer has a number average molecular weight in the range of about 700 to about 10,000, and preferably in the range of about 700 to about 4,000, as determined by vapor pressure osmometry.
The cloud point depressant additive of this invention typically encompasses a mixture of hydrocarbon substituents of varying carbon number within the recited range, and encompasses straight and branched chain moieties.
It has also been found that an additive of the structure
Figure US06342081-20020129-C00005
wherein R has at least 80% by weight of a hydrocarbon substituent from about 14 to about 16 carbons, R′ has at least 80% by weight of a hydrocarbon substituent from 16 to 18 carbons, and n is from about 2 to about 17, also has cloud point depressant properties. Preferably R has at least 90% by weight of a hydrocarbon substituent from about 14 to about 16 carbons, and most preferably R has at least 95% by weight of a hydrocarbon substituent from about 14 to about 16 carbons. Typically, R′ has at least 90% by weight of a hydrocarbon substituent from 16 to 18 carbons. The above additive, described as a polyimide, has a number average molecular weight as determined by vapor pressure osmometry in the range of about 1,200 to about 10,000, and preferably in the range of about 1,200 to about 5,000.
In addition, it has been found that certain ethylene vinyl acetate isobutylene terpolymers demonstrate cloud point depressant properties both alone and in combination with one or more of the above maleic anhydride α-olefin copolymer or polyimide additives. Useful ethylene vinyl acetate isobutylene terpolymers have a weight average molecular weight in the range of about 1,500 to about 18,000, a number average molecular weight in the range of about 400 to about 3,000, and a ratio of weight average molecular weight to number average molecular weight from about 1.5 to about 6. Preferably the weight average molecular weight ranges from about 3,000 to about 12,000, and the number average molecular weight ranges from about 1,500 to about 2,500. The terpolymers have a Brookfield viscosity in the range of about 100 to about 300 centipoise at 140° C. Typically the Brookfield viscosity is in the range of about 100 to about 200 centipoise. Vinyl acetate content is from about 25 to about 55 weight percent. Preferably the vinyl acetate content ranges from about 30 to about 45 weight percent; more preferably the vinyl acetate content ranges from about 35 to about 45 weight percent. The branching index is from 2 to 15, and preferably 5 to 10. The rate of isobutylene introduction depends on the rate of vinyl acetate introduction, and may range from about 0.01 to about 10 times the rate of vinyl acetate monomer flow rate to the reactor.
A fuel will cool to its cloud point generally in a static environment, such as storage tanks, shipping tanks or even fuel tanks where no separate agitation is supplied. However, a fuel will become cloudy even in a dynamic environment such as a moving fuel tank at sufficiently low temperature. To replicate the conditions which promote formation of a cloud point and permit evaluation of additives, ASTM D 2500 for measuring cloud point formation or ASTM D 3117 for measuring the wax appearance point, both incorporated herein by reference, can be utilized.
Optionally, the maleic anhydride α-olefin copolymer or polyimide can be combined with an ethylene vinyl acetate isobutylene terpolymer or ethylene vinyl acetate copolymer to produce a cloud point depressant additive combination which also provides cold flow improvement without adversely affecting the cloud point depressant properties.
The maleic anhydride α-olefin copolymer or polyimide additives of the present invention act as cloud point depressants when effective amounts are added to distillate fuels. Useful amounts of the additives range from about 50 to about 1,500 ppm by weight of the fuel being treated. Preferred amounts of the additives to improve cloud point depressant properties range from about 250 to about 500 ppm by weight of treated fuel. Maleic anhydride α-olefin copolymers and polyimides used according to the teachings of this invention may be derived from α-olefin products such as those manufactured by Chevron Corporation and identified as Gulftene® 18 Alpha-Olefin, or the like.
Useful amounts of the terpolymers range from about 10 to about 1,000 ppm by weight of the fuel being treated. Preferred amounts of terpolymers range from about 25 to about 250 ppm by weight of treated fuel in connection with improving cloud point depression.
The additives of this invention may be used as the sole additive in a distillate fuel. Also, the polyimide or maleic anhydride α-olefin copolymers may be used in combination with one or more terpolymers or copolymers as described above. In addition, cloud point depressant additives of this invention may be used in combination with other fuel additives such as corrosion inhibitors, antioxidants, sludge inhibitors, cold flow improvers, wax anti-settling agents, and the like.
OPERATING EXAMPLES
The following detailed operating examples illustrate the practice of the invention in its most preferred form, thereby enabling a person of ordinary skill in the art to practice the invention. The principles of this invention, its operating parameters and other obvious modifications thereof, will be understood in view of the following detailed procedure.
In evaluating cloud point performance the additive combinations described below were combined with a variety of diesel fuels at a weight concentration of about 50-1,500 ppm additive combination in the fuel, preferably 250-500 ppm additive combination in the fuel. Higher additive concentrations tend to impart additional cloud point depression effects to the fuel; however, the rate of improvement is lower at concentration levels above about 500 ppm when compared to the rate of improvement at levels below about 500 ppm. In all evaluations herein the additive or additive combination was combined with the fuel from a concentrate. One part of a 1:1 weight mixture of additive and xylene was combined with 19 parts by weight of the fuel to be evaluated to prepare the concentrate. The actual final weight concentration of additive in the fuel was adjusted by varying the appropriate amount of the concentrate added to the fuel. If more than one additive was incorporated into the fuel, individual additive concentrates were mixed into the fuel substantially at the same time.
It has been found that the effectiveness of maleic anhydride α-olefin copolymer and polyimide as cloud point depressant additives is related to the structure of the additive. The α-olefin used in making the above additives is a mixture of individual α-olefins having a range of carbon numbers. The starting α-olefin used to prepare both the maleic anhydride olefin copolymer and polyimide additives of the invention has at least a minimum concentration by weight which has a carbon number within the range from about C16 to about C18. The substituent “R” in the above formulas will have carbon numbers which are two carbons less than the α-olefin length, two of the α-olefin carbons becoming part of the polymer chain directly bonded to the repeating maleic anhydride or polyimide rings. Generally, α-olefins are not manufactured to a single carbon chain length, and thus the manufactured product will consist of component portions of individual α-olefins of varying carbon chain length. In addition, the substituent “R′” used in the polyimide cloud point additive will also have a minimum concentration within a range of carbon numbers.
Tallow amine is useful to introduce the R′ substituent in connection with polyimide manufacture, and is generally derived from tallow fatty acid. Thus, the range and percentage of carbon numbers for the components of the tallow amine will generally be those of tallow fatty acid. Tallow fatty acid is generally derived from beef tallow or mutton tallow. Though the constituent fatty acids may vary substantially in individual concentration in the beef tallow or mutton tallow based on factors such as source of the tallow, treatment and age of the tallow, general values have been generated and are provided in the table below. The values are typical rather than average.
TALLOW COMPOSITION TABLE
Constituent Fatty Acids (g/100 g Total Fatty Acids)
Saturated Unsaturated
Myristic Palmitic Stearic Oleic Linoleic
Fat (C14 ) (C16) (C18) (C18:1) (C18:2)
Beef Tallow 6.3 27.4 14.1 49.6 2.5
Mutton Tallow 4.6 24.6 30.5 36.0 4.3
Source: CRC Handbook of Chemistry and Physics, 74th ed. (1993-1994); p. 7-29.
The fatty acids from beef or mutton tallow can also be hydrogenated to lower the degree of unsaturation. Thus a tallow amine may contain a major portion by weight of unsaturated amine molecules, and alternatively with sufficient hydrogenation treatment may contain virtually no unsaturated amine molecules. Even with variations in tallow amine composition referred to above it is expected that the concentration by weight of hydrocarbon substituents from 16 to 18 carbons will be at least 80% by weight, and typically at least 90% by weight.
The following table lists maleic anhydride α-olefin copolymer and polyimide additives with their carbon number distributions for the various substituents of the additives tested. The percentages by weight of the carbon number ranges for the starting α-olefins were determined by using a Hewlett Packard HP-5890 gas chromatograph with a Chrompack WCOT (wool coated open tubular) Ulti-Metal 10 m×0.53 mm×0.15 μm film thickness column, with an HT SIMDIST CB coating. The sample was introduced via on-column injection onto the column as a solution in toluene. The gas chromatograph was equipped with a hydrogen flame ionization detector. A temperature program was activated to sequentially elute individual isomers. Because two carbons of the α-olefin become part of the polymer chain directly bonded to the repeating maleic anhydride or polyimide rings, the listed ranges for the “R” substituent shown in Table 1 are two carbons lower than the actual range determined chromatographically. Also, the listed ranges may encompass isomers having the same carbon number.
TABLE 1
R Substituent (% By Weight)2 R′ Substituent
Additive C12 C14 C16 C18 C22-26 C28-38 C40-48 C50-58 C60-76 H C16 C18 n
Polyimide I 1.3 98.4 0.3 26.01 68.51 2.95
Polyimide II 99.3 0.6 100
Polyimide III 80.5 14    3.2 1.8 0.4 100
Polyimide IV 12.3 58.5 15.9 10   3.3 26.01 68.51 1.13
Polyimide V 12.3 58.5 15.9 10   3.3 100
Maleic Copolymer I 1.3 98.4 0.3 4.1 
Maleic Copolymer II 99.3 0.6 100 10.6 
Maleic Copolymer III 12.3 58.5 15.9 10   3.3 3.41
Maleic Copolymer IV 80.5 14    3.2 1.8 0.4 3.6 
Maleic Copolymer V 24.8 0.5 24.6 0.1 23.2 18.1  4.8 3.0 0.9 5.4 
1Average representative figures, based on Tallow Composition Table.
2Total weight may not be 100% as a result of the presence of trace amounts of other materials, and rounding for calculation purposes.
The copolymers and terpolymers utilized individually in preparing the various additive combinations are characterized in Table 2 set out below.
TABLE 2
Vinyl
Viscosity @ Acetate
140° C. Content Mw
Additive (cP) (wt. %) Mn Mw Mn
Terpolymer I 125 37 2,237 11,664 5.2
Terpolymer II 190 42 1,902  3,326 1.7
Terpolymer III 135 45 2,067  6,438 3.1
Copolymer I 115 32 1,889  3,200  1.69
Fuels included in the evaluation of additives for cloud point depression performance are listed below in Table 3, which provides distillation data for the respective fuels according to test method ASTM D 86. The data indicate the boiling point temperature (° C.) at which specified volume percentages of the fuel have been recovered from the original pot contents at atmospheric pressure.
TABLE 3
Percentage Distilled/Temperature (° C.)
Initial Final %
Fuel B.P. 5% 10% 20% 30% 40% 50% 60% 70% 80% 90% 95% B.P. Residue
1 222 239 244 251 260 268 274 283 293 305 322 334 356 0.2
2 178 204 213 226 237 249 259 270 283 297 314 327 352 0.6
3 183 217 231 249 262 272 282 292 303 314 336 354 357 0.1
4 193 206 216 243 255 266 278 284 292 308 332 336 346 1.4
5 196 214 229 246 257 267 273 287 298 309 323 336 356 0.8
6 173 198 211 228 241 253 263 273 284 297 313 325 352 0.2
7 219 227 236 245 253 263 276 289 304 320 338 347 370 1.0
8 167 202 222 244 255 264 274 284 297 310 328 338 367 1.6
9 186 201 208 226 238 252 263 276 290 307 333 351 364 1.0
10  194 206 218 230 238 256 268 282 296 311 337 353 356 1.6
To evaluate whether the diesel fuels listed in Table 3 would be considered hard to treat, the temperature difference between the 20% distilled and 90% distilled temperatures (90-20%), and 90% distilled temperature and final boiling point (90%-FBP) were calculated. Also, the final boiling point was included. The data are provided in Table 4. A 90-20% temperature difference of about 100°-120° C. for a middle distillate cut fuel is considered normal; a difference of about 70°-100° C. is considered narrow and hard to treat; and a difference of less than about 70° C. is considered extreme narrow and hard to treat. A 90%-FBP temperature difference in the range of about 25° C. to about 35° C. is considered normal; a difference of less than about 25° C. is considered narrow and hard to treat; and a difference of more than about 35° C. is considered hard to treat. A final boiling point below about 360° C. or above about 380° C. is considered hard to treat. Distillation data were generated by utilizing the ASTM D 86 test method. Additional disclosure on hard-to-treat fuels is found in U.S. Pat. No. 5,681,359, incorporated herein by reference.
TABLE 4
Temperature Difference (° C.)
Fuel 90%-20% 90%-FBP FBP (° C.)
1 71 34 356
2 88 38 352
3 87 21 357
4 89 14 346
5 77 33 356
6 85 39 352
7 93 32 370
8 84 39 367
9 107  31 364
10  107  19 356
If the fuel met at least one of the above three evaluation parameters, i.e., 90%-20% distilled temperature difference, 90%-final boiling point distilled temperature difference, or final boiling point, it was considered hard to treat. Based on the evaluation parameters and the data in Tables 3 and 4, fuels 1 through 8 and 10 are considered hard to treat, and fuel 9 is considered normal. As the following examples demonstrate, the cloud point additives of the invention have beneficial effects when used with both normal and hard-to-treat fuels.
EXAMPLE 1
The cloud points of three fuel compositions were compared. The fuel used in preparing each of the compositions was Fuel 1. The first fuel composition contained no added cloud point depressant. The second fuel composition included 500 ppm by weight of Polyimide I. The third fuel composition included 500 ppm by weight of Maleic Copolymer I. The results are set out in Table 5.
TABLE 5
Cloud Point
Additive ° C. ° F.
 −7 19.4°
Polyimide I −13  8.6°
Maleic Copolymer I −10   14°
EXAMPLE 2
The effect of change in concentration of cloud point depressant additive on the cloud point was evaluated using Fuel 2. The two additives tested above in Example 1 were separately combined with Fuel 2 and evaluated for cloud point depressant effect at additive concentrations of 500 ppm and 1000 ppm by weight. The cloud point temperatures are set out in Table 6.
TABLE 6
Concentration Cloud Point
Additive (ppm) ° C. ° F.
1) — −13 8.6
2) Polyimide I  500 −19 −2.2
2a) Polyimide I 1,000 −20 −4
3) Maleic Copolymer I  500 −15 5
3a) Maleic Copolymer I 1,000 −16 3.2
An improvement was observed by using 1,000 ppm additive when compared with the same additive at a 500 ppm concentration level. However, the change in cloud point from 500 ppm to 1,000 ppm additive level was not as great as the cloud point change from 0 ppm to 500 ppm additive level for both Polyimide I and Maleic Copolymer I.
Example 3
The cloud point depressant effect of the two additives tested in Examples 1 and 2 was evaluated on other distillate fuels when introduced at a concentration of 500 ppm by weight. The results are set out below in Table 7.
TABLE 7
Cloud Point
Fuel Additive ° C. ° F.
3 −10 14
3 Polyimide I −15 5
3 Maleic Copolymer I   −11.5 11.3
4 −11 12.2
4 Polyimide I −15 5
4 Maleic Copolymer I −13 8.6
EXAMPLE 4
To evaluate the effect of substituent chain length on the ability of the additive to lower the cloud point, a number of additive compositions were added to Fuel 1 and Fuel 3 at a concentration of 500, ppm by weight. The compositions of the tested additives are set.out in Table 1 above. The additives and test results are provided below in Table 8.
TABLE 8
Cloud Point
Fuel Composition Fuel Composition
Additive [Fuel 1] [Fuel 3]
(500 ppm by wt.) ° C. ° F. ° C. ° F.
−7 19.4 −10 14  
Polyimide I −13  8.6 −15  5  
Maleic Copolymer I −10  14 −11.5 11.3
Maleic Copolymer II −9 15.8 −8 17.6
Maleic Copolymer III −9 15.8 −11 12.2
Maleic Copolymer IV −7 19.4 −12 10.4
Maleic Copolymer V −10  14 −10.8 12.6
Polyimide II −8 17.6 −11 12.2
Polyimide III −8 17.6 −11 12.2
Polyimide IV −8 17.6 −11 12.2
Polyimide V −9 15.8 −7 19.4
As the above data indicate, the extent of the cloud point depressant effect will vary with the fuel to be treated. Polyimide I and Maleic Copolymer I demonstrated good cloud point depressant efficacy with both Fuels 1 and 3. The cloud point depressant effect of the remaining additives in Table 8 was generally not as significant nor as uniform with both Fuels 1 and 3 as was observed with Polyimide I and Maleic Copolymer I.
EXAMPLE 5
To demonstrate the utility of a cloud point depressant additive used with a variety of fuels, several of which are classified as hard-to-treat, Polyimide I was incorporated into a number of different fuels at 500 ppm concentration by weight and evaluated for cloud point depressant effect. The results of this evaluation are provided in Table 9 below.
TABLE 9
CLOUD POINT
With 500 ppm
Untreated Polyimide I
Fuel ° C. ° F. ° C. ° F.
4 −11 12.2 −15 5
5 −11 12.2 −13 8.6
6 −10 14 −18 −0.4
7  −9 15.8 −14 6.8
8 −10 14 −14 6.8
9 −10 14 −15 5
10  −13 8.6 −17 1.4
As the data indicate, Polyimide I at 500 ppm concentration in Fuels 4 through 10 produced a cloud point depressant effect up to 8° C. Celsius over the group of fuels, and typically at least 4° Celsius.
EXAMPLE 6
To evaluate the effect of an ethylene vinyl acetate isobutylene terpolymer on the cloud point of a distillate fuel, several fuels were combined with 500 ppm terpolymer or copolymer additive and measured for cloud point. The results of this evaluation are provided in Table 10 below.
TABLE 10
CLOUD POINT
Fuel Additive (500 ppm by wt.) °C. °F.
1 −7 19.4
1 Terpolymer I − 10 14
1 Terpolymer III − 11 12.2
1 Copolymer I − 6 21.2
3 − 10 14
3 Terpolymer I − 12 10.4
3 Terpolymer II − 12 10.4
3 Copolymer I − 11 12.2
7 − 9 15.8
7 Terpolymer II − 11 12.2
7 Terpolymer III − 11 12.2
8 − 10 14
8 Terpolymer III − 12 10.4
Generally, incorporation of a terpolymer additive to the respective fuels resulted in a demonstrable cloud point depressant effect. Incorporation of a copolymer additive either had the undesirable effect of raising the cloud point, or of providing a less substantial positive effect on cloud point depression compared to the terpolymer additives tested.
EXAMPLE 7
In formulating additive packages for modifying more than one property of a fuel, the effect of one additive may not positively correlate to that of another additive. Thus, an additive incorporated to improve one property of a fuel may have an adverse effect on another property of the fuel.
It has been found that an ethylene vinyl acetate copolymer or an ethylene vinyl acetate isobutylene terpolymer, which can be used to improve the cold flow properties of the fuel, combined with a polyimide or maleic anhydride α-olefin copolymer of the invention generally does not have an antagonistic effect on either the cloud point or cold flow characteristics of the fuel. In this evaluation, an additive package consisting of 500 ppm by weight of a 1:1 mixture of either copolymer or terpolymer and polyimide I was combined with a variety of fuels and measured for cloud point depression. The additive package combinations and cloud point measurements are set out in Table 11 below.
TABLE 11
Cloud Point
Fuel Additive (by weight) °C. °F.
1 −7 19.4
1 250 ppm TerpolymerI/250 −12 10.4
ppm Polyimide I
1 250 ppm TerpolymerIII/250 −11 12.2
ppm Polyimide I
1 250 ppm CopolymerI/250 −9 15.8
ppm Polyimide I
2 −13 8.6
2 250 ppm CopolymerI/250 −17 1.4
ppm Polyimide I
2 250 ppm CopolymerI/500 −17 1.4
ppm Polyimide I
2 250 ppm TerpolymerI/250 −17 1.4
ppm Polyimide I
2 250 ppm TerpolymerI/500 −19 −2.2
ppm Polyimide I
To evaluate the effect of this type of additive combination on fuel cold flow, several additive combinations were tested for Cold Filter Plugging Point (CFPP), IP 309, incorporated herein by reference, or pour point, ASTM D 97, also incorporated herein by reference. Specifically Fuel 2 both without additives and with certain additive combinations was tested for CFPP and pour point. Without additives the CFPP of Fuel 2 was −15.5° C. Incorporation of 250 ppm Copolymer I and 250 ppm Polyimide I into Fuel 2 improved the CFPP to −22° C.
The pour point of Fuel 2 was −21° C. without additive. Incorporation of 250 ppm Copolymer I and 500 ppm Polyimide I improved the pour point to −44° C., and incorporation of 250 ppm Terpolymer I and 500 ppm Polyimide I improved the pour point to −50° C.
EXAMPLE 8
Several fuel compositions containing cloud point depressant additives were evaluated for low temperature flow performance utilizing the Low Temperature Flow Test (LTFT), ASTM D 4539, incorporated herein by reference. This test estimates the filterability of diesel fuels in some automotive equipment at low temperatures. Broadly, the test involves cooling the fuel to be tested to a temperature initially at least 5% above the wax appearance point (ASTM D 3117) or the cloud point (ASTM D 2500). After the sample has cooled to the desired temperature the sample is gently stirred to disperse any settled wax crystals and then drawn through a filter under vacuum. The sample passes at a given test temperature if at least 180 milliliters of sample passes through the filter within sixty seconds.
In the test, three fuels were evaluated, each containing 500 ppm Polyimide I as the additive. Cloud point and LTFT data are provided in Table 12 below.
TABLE 12
Cloud LTFT (°C.)
Fuel Additive Point (°C.) Passed Failed
1 500 ppm Polyimide I −13 −14 −15
3 500 ppm Polyimide I −15 −17 −18
9 500 ppm Polyimide I −15 −20 Unknown1
1The test system employed a low end temperature limit of −20° C. The sample required 18 seconds to pass the required quantity of fuel at this temperature limit. The ultimate failure temperature for this composition would be lower than −20°
The data demonstrates that the passed LTFT values for the tested fuel compositions containing additive were consistently lower than the respective cloud points of these compositions.
As the above examples demonstrate, the additives of the invention provide substantial improvements in the cloud point properties of distillate fuels relative to the unmodified fuel. The improvement in cloud point depression extends to both normal and hard-to-treat fuels. These additives may be used in combination with other fuel additives, such as those for improving flow properties to enhance the operability of the fuel by encompassing the cloud point depression improvement as well as the properties improved by incorporation of the other additives.
Thus it is apparent that there has been provided, in accordance with the invention, a cloud point depressant additive and fuel composition which fully satisfies the objects, aims, and advantages set forth above. While the invention has been described in conjunction with specific embodiments thereof, it is evident that many alternatives, modifications, and variations will be apparent to those skilled in the art in light of the foregoing description. Accordingly, departures may be made from such details without departing from the spirit or scope of the general inventive concept.

Claims (7)

What is claimed is:
1. A distillate fuel composition having improved cloud point depressant properties comprising a major proportion of a distillate fuel and an amount of about 250 ppm to about 1,500 ppm of a maleic anhydride α-olefin copolymer having the formula:
Figure US06342081-20020129-C00006
wherein R has at least 80% by weight of a hydrocarbon substituent from about 14 to about 16 carbons, and n is from about 2 to about 30.
2. The composition of claim 1 wherein said distillate fuel is a middle distillate fuel.
3. The composition of claim 1 wherein said distillate fuel is No. 2 diesel fuel.
4. The composition of claim 1 wherein said distillate fuel is hard-to-treat fuel.
5. The composition of claim 1 wherein said maleic anhydride α-olefin copolymer is derived from substantially equimolar proportions of maleic anhydride and α-olefin.
6. The composition of claim 1 wherein at least 90% by weight of the R group of the copolymer is a C13 to C16 hydrocarbon.
7. The composition of claim 1 wherein at least 95% by weight of the R group of the copolymer is a C14 to C16 hydrocarbon.
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US6673131B2 (en) 2002-01-17 2004-01-06 Equistar Chemicals, Lp Fuel additive compositions and distillate fuels containing same
CN110387002A (en) * 2018-04-23 2019-10-29 广州精至百特利化工科技有限公司 A kind of preparation of industrial oleic acid pour-point depressant and its application method

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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GB9826448D0 (en) * 1998-12-02 1999-01-27 Exxon Chemical Patents Inc Fuel oil additives and compositions
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AU2017335817B2 (en) * 2016-09-29 2021-11-11 Ecolab Usa Inc. Paraffin inhibitors, and paraffin suppressant compositions and methods
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US11352550B2 (en) * 2019-05-21 2022-06-07 Plus5, Inc. Method for paraffin inhibiting
US20230120367A1 (en) * 2021-10-14 2023-04-20 Ecolab Usa Inc. Antifouling agents for plastic-derived synthetic feedstocks

Citations (47)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE254284C (en)
US2615845A (en) * 1948-08-02 1952-10-28 Standard Oil Dev Co Lubricating oil additives
US2698316A (en) * 1949-11-14 1954-12-28 Socony Vacuum Oil Co Inc Amine derivatives of copolymers of alpha, beta-unsaturated polycarboxylic acids
US2977334A (en) 1956-10-04 1961-03-28 Monsanto Chemicals Derivatives of ethylene/maleic anhydride copolymers
US3048479A (en) 1959-08-03 1962-08-07 Exxon Research Engineering Co Ethylene-vinyl ester pour depressant for middle distillates
US3250599A (en) 1962-12-03 1966-05-10 Sinclair Research Inc Fuels of improved low temperature pumpability
US3382056A (en) * 1966-06-03 1968-05-07 Chevron Res Maleic anhydride copolymers as rust inhibitors
US3413104A (en) * 1964-12-10 1968-11-26 Chevron Res Imides of olefin-maleic anhydride copolymers as diesel fuel additives
US3444082A (en) 1966-02-07 1969-05-13 Chevron Res Acid-amide pour point depressants
US3458295A (en) * 1965-10-12 1969-07-29 Chevron Res Corrosion inhibitors
US3462249A (en) 1967-03-31 1969-08-19 Exxon Research Engineering Co Fuel oil compositions containing grafted polymers
US3471458A (en) 1966-12-16 1969-10-07 Chevron Res Polyimides of olefin-maleic anhydride copolymers as diesel fuel additives
DE1940944A1 (en) 1968-08-29 1970-03-05 Mobil Oil Corp Hydrocarbon mixtures with improved fluidity
US3560456A (en) 1969-05-26 1971-02-02 Gulf Research Development Co Process of forming copolymers of maleic anhydride and an aliphatic olefin having from 16 to 18 carbon atoms
US3620696A (en) 1968-09-17 1971-11-16 Exxon Research Engineering Co Fuel oil with improved flow properties
US3677725A (en) * 1970-02-04 1972-07-18 Mobil Oil Corp Liquid hydrocarbon compositions containing antistatic agents
US3694176A (en) 1968-04-01 1972-09-26 Exxon Research Engineering Co Polymers comprising ethylene and ethylenically unsaturated dicarboxylic acids or esters thereof,and oil compositions containing said polymers
GB1374051A (en) 1971-02-16 1974-11-13 Exxon Research Engineering Co Middle distillate compositions with filterability and flow properties
US3854893A (en) 1972-06-14 1974-12-17 Exxon Research Engineering Co Long side chain polymeric flow improvers for waxy hydrocarbon oils
US3909215A (en) * 1973-03-27 1975-09-30 Chevron Res Rust inhibitors for hydrocarbon fuels
US3966428A (en) 1973-10-31 1976-06-29 Exxon Research And Engineering Company Ethylene backbone polymers in combination with ester polymers having long alkyl side chains are low viscosity distillate fuel cold flow improvers
US4151069A (en) 1974-10-17 1979-04-24 Exxon Research & Engineering Co. Olefin-dicarboxylic anhydride copolymers and esters thereof are dewaxing aids
US4178951A (en) 1978-10-10 1979-12-18 Texaco Inc. Low pour point crude oil compositions
US4178950A (en) 1978-10-10 1979-12-18 Texaco Inc. Residual fuel compositions with low pour points
US4240916A (en) 1976-07-09 1980-12-23 Exxon Research & Engineering Co. Pour point depressant additive for fuels and lubricants
JPS5646096A (en) 1979-09-18 1981-04-27 Sumikin Kokan Koji Kk Propelling method employing resin concrete wrapped steel pipe
EP0030099A1 (en) 1979-11-23 1981-06-10 Exxon Research And Engineering Company Additive combinations and fuels containing them
JPS5672942A (en) 1979-11-17 1981-06-17 Yamashiro Seiki Seisakusho:Kk Injection molding device for testing resin material
GB1593672A (en) 1977-10-07 1981-07-22 Exxon Research Engineering Co Polymer combinations useful in distillate hydrocarbon oils to improve cold flow properties
US4402845A (en) 1981-05-26 1983-09-06 Texaco Inc. Process for improving the spreadability of marine diesel cylinder oils
US4537601A (en) * 1982-05-17 1985-08-27 Petrolite Corporation Antistats containing acrylonitrile copolymers and polyamines
JPS61117188A (en) 1984-11-13 1986-06-04 日本化薬株式会社 Electric primer and initiation
EP0196217A2 (en) 1985-03-25 1986-10-01 Amoco Corporation Ethylene-unsaturated, ester-substituted olefin terpolymer flow improvers
JPS62249860A (en) 1986-04-23 1987-10-30 Watanabe Takeshi Tape cutting device
US4863486A (en) 1984-02-21 1989-09-05 Exxon Chemical Patents Inc. Middle distillate compositions with improved low temperature properties
US4862908A (en) 1986-07-17 1989-09-05 Ruhrchemie Aktiengesellschaft Mineral oils and mineral oil distillates having improved flowability and method for producing same
US4882034A (en) 1987-03-18 1989-11-21 Exxon Chemical Patents Inc. Crude oil or fuel oil compositions
US4900332A (en) 1987-04-01 1990-02-13 Institut Francais Du Petrole Nitrogenous copolymers, their preparation and use as additives for improving the pour properties of hydrocarbon middle distillates
US4985048A (en) 1987-12-16 1991-01-15 Hoechst Aktiengesellschaft Polymer mixtures for improving the low-temperature flow properties of mineral oil distillates
US5011505A (en) 1987-09-02 1991-04-30 Exxon Chemical Patents Inc. Flow improvers and cloud point depressants
US5080686A (en) * 1982-10-20 1992-01-14 Petrolite Corporation Alkyl or alkenyl succinic acids as corrosion inhibitors for oxygenated fuels
US5189231A (en) 1990-04-30 1993-02-23 Societa' Italiana Additivi Per Carburanti S.R.L. Compositions of liquid hydrocarbons from refining endowed with improved behavior at low temperatures
US5256166A (en) 1984-12-06 1993-10-26 National Distillers And Chemical Corporation Terpolymer of ethylene, vinyl acetate and isobutylene useful as pour point depressants in distillate oils
EP0654526A2 (en) 1993-11-09 1995-05-24 The Lubrizol Corporation Cloud point depressant composition
US5525128A (en) 1990-01-31 1996-06-11 Exxon Chemical Patents Inc. Fuel oil additives and compositions
US5681359A (en) 1996-10-22 1997-10-28 Quantum Chemical Corporation Ethylene vinyl acetate and isobutylene terpolymer as a cold flow improver for distillate fuel compositions
US5766273A (en) * 1994-08-26 1998-06-16 Basf Aktiengesellschaft Polymer blends and their use as additives for mineral oil middle distillates

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2542542A (en) * 1948-08-02 1951-02-20 Standard Oil Dev Co Lubricating oil additives
US4659334A (en) * 1984-07-10 1987-04-21 Petrolite Corporation Particulate compositions used in petroleum systems comprising encapsulated materials
US4992080A (en) * 1988-10-31 1991-02-12 Conoco Inc. Oil compositions containing alkyl amine derivatives of copolymers of an alpha olefin or an alkyl vinyl ether and an unsaturated alpha, beta-dicarboxylic compound
US5214224A (en) * 1992-07-09 1993-05-25 Comer David G Dispersing asphaltenes in hydrocarbon refinery streams with α-olefin/maleic anhydride copolymer
US6203583B1 (en) * 1999-05-13 2001-03-20 Equistar Chemicals, Lp Cold flow improvers for distillate fuel compositions

Patent Citations (49)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE254284C (en)
US2615845A (en) * 1948-08-02 1952-10-28 Standard Oil Dev Co Lubricating oil additives
US2698316A (en) * 1949-11-14 1954-12-28 Socony Vacuum Oil Co Inc Amine derivatives of copolymers of alpha, beta-unsaturated polycarboxylic acids
US2977334A (en) 1956-10-04 1961-03-28 Monsanto Chemicals Derivatives of ethylene/maleic anhydride copolymers
US3048479A (en) 1959-08-03 1962-08-07 Exxon Research Engineering Co Ethylene-vinyl ester pour depressant for middle distillates
US3250599A (en) 1962-12-03 1966-05-10 Sinclair Research Inc Fuels of improved low temperature pumpability
US3413104A (en) * 1964-12-10 1968-11-26 Chevron Res Imides of olefin-maleic anhydride copolymers as diesel fuel additives
US3458295A (en) * 1965-10-12 1969-07-29 Chevron Res Corrosion inhibitors
US3444082A (en) 1966-02-07 1969-05-13 Chevron Res Acid-amide pour point depressants
US3382056A (en) * 1966-06-03 1968-05-07 Chevron Res Maleic anhydride copolymers as rust inhibitors
US3471458A (en) 1966-12-16 1969-10-07 Chevron Res Polyimides of olefin-maleic anhydride copolymers as diesel fuel additives
US3462249A (en) 1967-03-31 1969-08-19 Exxon Research Engineering Co Fuel oil compositions containing grafted polymers
US3694176A (en) 1968-04-01 1972-09-26 Exxon Research Engineering Co Polymers comprising ethylene and ethylenically unsaturated dicarboxylic acids or esters thereof,and oil compositions containing said polymers
DE1940944A1 (en) 1968-08-29 1970-03-05 Mobil Oil Corp Hydrocarbon mixtures with improved fluidity
GB1245879A (en) 1968-08-29 1971-09-08 Mobil Oil Corp Fluidity improvers
US3620696A (en) 1968-09-17 1971-11-16 Exxon Research Engineering Co Fuel oil with improved flow properties
US3560456A (en) 1969-05-26 1971-02-02 Gulf Research Development Co Process of forming copolymers of maleic anhydride and an aliphatic olefin having from 16 to 18 carbon atoms
US3677725A (en) * 1970-02-04 1972-07-18 Mobil Oil Corp Liquid hydrocarbon compositions containing antistatic agents
GB1374051A (en) 1971-02-16 1974-11-13 Exxon Research Engineering Co Middle distillate compositions with filterability and flow properties
US3854893A (en) 1972-06-14 1974-12-17 Exxon Research Engineering Co Long side chain polymeric flow improvers for waxy hydrocarbon oils
US3909215A (en) * 1973-03-27 1975-09-30 Chevron Res Rust inhibitors for hydrocarbon fuels
US3966428A (en) 1973-10-31 1976-06-29 Exxon Research And Engineering Company Ethylene backbone polymers in combination with ester polymers having long alkyl side chains are low viscosity distillate fuel cold flow improvers
US4151069A (en) 1974-10-17 1979-04-24 Exxon Research & Engineering Co. Olefin-dicarboxylic anhydride copolymers and esters thereof are dewaxing aids
US4240916A (en) 1976-07-09 1980-12-23 Exxon Research & Engineering Co. Pour point depressant additive for fuels and lubricants
GB1593672A (en) 1977-10-07 1981-07-22 Exxon Research Engineering Co Polymer combinations useful in distillate hydrocarbon oils to improve cold flow properties
US4178950A (en) 1978-10-10 1979-12-18 Texaco Inc. Residual fuel compositions with low pour points
US4178951A (en) 1978-10-10 1979-12-18 Texaco Inc. Low pour point crude oil compositions
JPS5646096A (en) 1979-09-18 1981-04-27 Sumikin Kokan Koji Kk Propelling method employing resin concrete wrapped steel pipe
JPS5672942A (en) 1979-11-17 1981-06-17 Yamashiro Seiki Seisakusho:Kk Injection molding device for testing resin material
EP0030099A1 (en) 1979-11-23 1981-06-10 Exxon Research And Engineering Company Additive combinations and fuels containing them
US4402845A (en) 1981-05-26 1983-09-06 Texaco Inc. Process for improving the spreadability of marine diesel cylinder oils
US4537601A (en) * 1982-05-17 1985-08-27 Petrolite Corporation Antistats containing acrylonitrile copolymers and polyamines
US5080686A (en) * 1982-10-20 1992-01-14 Petrolite Corporation Alkyl or alkenyl succinic acids as corrosion inhibitors for oxygenated fuels
US4863486A (en) 1984-02-21 1989-09-05 Exxon Chemical Patents Inc. Middle distillate compositions with improved low temperature properties
JPS61117188A (en) 1984-11-13 1986-06-04 日本化薬株式会社 Electric primer and initiation
US5256166A (en) 1984-12-06 1993-10-26 National Distillers And Chemical Corporation Terpolymer of ethylene, vinyl acetate and isobutylene useful as pour point depressants in distillate oils
US4746327A (en) 1985-03-25 1988-05-24 Standard Oil Company (Indiana) Ethylene-unsaturated, ester-substituted olefin terpolymer flow improvers
EP0196217A2 (en) 1985-03-25 1986-10-01 Amoco Corporation Ethylene-unsaturated, ester-substituted olefin terpolymer flow improvers
JPS62249860A (en) 1986-04-23 1987-10-30 Watanabe Takeshi Tape cutting device
US4862908A (en) 1986-07-17 1989-09-05 Ruhrchemie Aktiengesellschaft Mineral oils and mineral oil distillates having improved flowability and method for producing same
US4882034A (en) 1987-03-18 1989-11-21 Exxon Chemical Patents Inc. Crude oil or fuel oil compositions
US4900332A (en) 1987-04-01 1990-02-13 Institut Francais Du Petrole Nitrogenous copolymers, their preparation and use as additives for improving the pour properties of hydrocarbon middle distillates
US5011505A (en) 1987-09-02 1991-04-30 Exxon Chemical Patents Inc. Flow improvers and cloud point depressants
US4985048A (en) 1987-12-16 1991-01-15 Hoechst Aktiengesellschaft Polymer mixtures for improving the low-temperature flow properties of mineral oil distillates
US5525128A (en) 1990-01-31 1996-06-11 Exxon Chemical Patents Inc. Fuel oil additives and compositions
US5189231A (en) 1990-04-30 1993-02-23 Societa' Italiana Additivi Per Carburanti S.R.L. Compositions of liquid hydrocarbons from refining endowed with improved behavior at low temperatures
EP0654526A2 (en) 1993-11-09 1995-05-24 The Lubrizol Corporation Cloud point depressant composition
US5766273A (en) * 1994-08-26 1998-06-16 Basf Aktiengesellschaft Polymer blends and their use as additives for mineral oil middle distillates
US5681359A (en) 1996-10-22 1997-10-28 Quantum Chemical Corporation Ethylene vinyl acetate and isobutylene terpolymer as a cold flow improver for distillate fuel compositions

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
Hihara et al., 91:195808d Fuel Oil Compositions, Chemical Abstracts, vol. 91, 1979.
Hihara et al., 91:213717e Fuel Oil Compositions, Chemical Abstracts, vol. 91, 1979.
Nishikawa, et al., 92:200767s Fuel Oil Compositions, Chemical Abstracts, vol. 91, 1979.

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6673131B2 (en) 2002-01-17 2004-01-06 Equistar Chemicals, Lp Fuel additive compositions and distillate fuels containing same
CN110387002A (en) * 2018-04-23 2019-10-29 广州精至百特利化工科技有限公司 A kind of preparation of industrial oleic acid pour-point depressant and its application method

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